605675-58-9

Upstream product

• 65-85-0 benzoic acid 
• 605675-52-3 (2R,3R,4R,6S)-3,4-di(benzyloxy)-2-benzyloxymethyl-1-azabicyclo[4.1.0]heptane 
• 850190-26-0 2-((1R,2R,3R)-2,3-Bis-benzyloxy-1-benzyloxymethyl-hex-5-enyl)-isoindole-1,3-dione 
• 850190-25-9 4-Nitro-benzoic acid (1S,2S,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-hex-5-enyl ester 
• 55628-54-1 3,4,6-tri-O-benzyl-D-glucal 
• 850190-27-1 (2R,3R,4R)-3,4-Bis-benzyloxy-2-benzyloxymethyl-6-iodomethyl-piperidine 
• 160549-11-1 3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranose 
• 605675-49-8 (2S,3R,4R)-1,3,4-Tris-benzyloxy-hept-6-en-2-ol 
• 605675-50-1 (1R,2R,3R)-2,3-Bis-benzyloxy-1-benzyloxymethyl-hex-5-enylamine 
• 157736-63-5 (2R,3R,4R)-1,3,4-Tris-benzyloxy-hept-6-en-2-ol 

Relevant academic research and scientific papers

General synthesis and biological evaluation of α-1-C-substituted derivatives of fagomine (2-deoxynojirimycin-α-C-glycosides)

A general synthesis of α-1-C-substituted derivatives of fagomine (2-deoxynojirimycin-α-C-glycosides) by ring-opening reactions of an aziridine with various heteroatomic nucleophiles, including thiol, amine, alcohol, carboxylate and phosphate, is described

Ring-opening reactions of iminosugar-derived aziridines: Application to the general synthesis of α-1-C-substituted derivatives of fagomine

A general approach to α-1-C-substituted derivatives of fagomine (2-deoxynojirimycin-α-C-glycosides) by ring-opening reactions of an aziridine with various heteroatomic nucleophiles, including thiol, amine, alcohol, carboxylate and phosphate, is reported.